Found 347 chains in Genus chains table. Displaying 1 - 50. Applied filters: Proteins

Search results query: Cyclin A; domain 1

Total Genus Sequence Length pdb Title
1003 3198 3vkgA X-ray structure of an mtbd truncation mutant of dynein motor domain
899 3218 3vkhA X-ray structure of a functional full-length dynein motor domain
807 2695 4ai6A Dynein motor domain - adp complex
804 2695 4akgA Dynein motor domain - atp complex
798 2695 4akhA Dynein motor domain - amppnp complex
798 2695 4akiA Dynein motor domain - luac derivative
16 114 1enwA Elongation factor tfiis domain ii
28 134 4by7X Elongating rna polymerase ii-bye1 tld complex
28 192 4bbsM Structure of an initially transcribing rna polymerase ii-tfiib complex
33 164 3po3S Arrested rna polymerase ii reactivation intermediate
60 263 2w2hA Structural basis of transcription activation by the cyclin t1-tat-tar rna complex from eiav
18 163 3gtmS Co-complex of backtracked rna polymerase ii with tfiis
21 134 4by1X Elongating rna polymerase ii-bye1 tld complex soaked with ampcpp
82 201 1d3uB Tata-binding protein/transcription factor (ii)b/bre+tata-box complex from pyrococcus woesei
65 193 1aisB Tata-binding protein/transcription factor (ii)b/tata-box complex from pyrococcus woesei
75 207 1c9bA Crystal structure of a human tbp core domain-human tfiib core domain complex bound to an extended, modified adenoviral major late promoter (admlp)
66 204 1volA Tfiib (human core domain)/tbp (a.thaliana)/tata element ternary complex
105 343 4rocA Human tfiib-related factor 2 (brf2) and tbp bound to u6#2 promoter
99 342 4rodA Human tfiib-related factor 2 (brf2) and tbp bound to trnau1 promoter
98 264 5lqfB Cdk1/cyclinb1/cks2 in complex with nu6102
94 258 5lmkB Structure of phopsho-cdk2-cyclin a in complex with an atp-competitive inhibitor
90 270 5l2wB The x-ray co-crystal structure of human cdk2/cycline and dinaciclib.
94 257 5if1B Crystal structure apo cdk2/cyclin a
93 268 5idpB Cdk8-cycc in complex with (3-amino-1h-indazol-5-yl)-[(s)-2-(4-fluoro-phenyl)-piperidin-1-yl]-methanone
93 266 5i5zB Cdk8-cycc in complex with 8-(1-methyl-2,2-dioxo-2,3-dihydro-1h-2l6-benzo[c]isothiazol-5-yl)-[1,6]naphthyridine-2-carboxylic acid methylamide
100 267 5icpB Cdk8-cycc in complex with [(s)-2-(4-chloro-phenyl)-pyrrolidin-1-yl]-(5-methyl-imidazo[5,1-b][1,3,4]thiadiazol-2-yl)-methanone
92 267 5hvyB Cdk8/cycc in complex with compound 20
93 266 5hbeB Cdk8-cycc in complex with 8-[3-chloro-5-(1-methyl-2,2-dioxo-2, 3-dihydro-1h-2l6-benzo[c]isothiazol-5-yl)-pyridin- 4-yl]-1-oxa-3,8-diaza-spiro[4.5]decan-2-one
90 241 5acbA Crystal structure of the human cdk12-cyclink complex
335 1059 4hntA Crystal structure of f403a mutant of s. aureus pyruvate carboxylase
97 262 4cfuB Structure-based design of c8-substituted o6-cyclohexylmethoxyguanine cdk1 and 2 inhibitors.
95 260 4cfxB Structure-based design of c8-substituted o6-cyclohexylmethoxyguanine cdk1 and 2 inhibitors.
97 258 5cyiB Cdk2/cyclin a covalent complex with 6-(cyclohexylmethoxy)-n-(4-(vinylsulfonyl)phenyl)-9h-purin-2-amine (nu6300)
104 268 5ceiB Crystal structure of cdk8:cyclin c complex with compound 22
91 266 5bnjB Cdk8/cycc in complex with 8-{3-chloro-5-[4-(1-methyl-1h-pyrazol-4-yl)-phenyl]-pyridin- 4-yl}-2,8-diaza-spiro[4.5]decan-1-one
349 1144 4hnvA Crystal structure of r54e mutant of s. aureus pyruvate carboxylase
57 206 4zgdB Mutant r157a of fe-type nitrile hydratase from comamonas testosteroni ni1
52 206 4zgeB Double mutant h80w/h81w of fe-type nitrile hydratase from comamonas testosteroni ni1
55 206 4zgjB Double mutant h80a/h81a of fe-type nitrile hydratase from comamonas testosteroni ni1
334 1059 4hnuA Crystal structure of k442e mutant of s. aureus pyruvate carboxylase
103 273 4z6yA Structure of the tbc1d7-tsc1 complex
99 267 4f7sB Crystal structure of human cdk8/cycc in the dmg-in conformation
97 268 4f7jB Crystal structure of human cdk8/cycc in complex with compound 3 (1-[3-tert-butyl-1-(4-methylphenyl)-1h-pyrazol-5-yl]-3-(2-hydroxyethyl)urea)
94 268 4f7nB Crystal structure of human cdk8/cycc in complex with compound 11 (1-[3-tert-butyl-1-(4-methylphenyl)-1h-pyrazol-5-yl]-3-(5-hydroxypentyl)urea)
100 266 4f6sB Crystal structure of human cdk8/cycc in complex with compound 7 (1-[3-tert-butyl-1-(4-methylphenyl)-1h-pyrazol-5-yl]urea)
85 266 4f7lB Crystal structure of human cdk8/cycc in complex with compound 2 (tert-butyl [3-({[3-tert-butyl-1-(4-methylphenyl)-1h-pyrazol-5-yl]carbamoyl}amino)propyl]carbamate)
98 267 4f6uB Crystal structure of human cdk8/cycc in complex with compound 5 (1-[3-tert-butyl-1-(4-methylphenyl)-1h-pyrazol-5-yl]-3-[3-(morpholin-4-yl)propyl]urea)
226 638 4eljA Crystal structure of the inactive retinoblastoma protein phosphorylated at t373
93 266 4f70B Crystal structure of human cdk8/cycc in complex with compound 4 (1-[3-tert-butyl-1-(4-methylphenyl)-1h-pyrazol-5-yl]-3-[2-(morpholin-4-yl)ethyl]urea)
100 267 4f6wB Crystal structure of human cdk8/cycc in complex with compound 1 (n-[3-tert-butyl-1-(4-methylphenyl)-1h-pyrazol-5-yl]-4-[2-({[3-tert-butyl-1-(4-methylphenyl)-1h-pyrazol-5-yl]carbamoyl}amino)ethyl]piperazine-1-carboxamide)